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GPD1L antibody (AA 1-351)

GPD1L Reactivity: Human WB, ELISA, ICC, IF Host: Mouse Monoclonal AT14E2 unconjugated
Catalog No. ABIN5776141
  • Target See all GPD1L Antibodies
    GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
    Binding Specificity
    • 8
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-351
    Reactivity
    • 28
    • 21
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 26
    • 2
    Mouse
    Clonality
    • 28
    Monoclonal
    Conjugate
    • 16
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GPD1L antibody is un-conjugated
    Application
    • 20
    • 12
    • 9
    • 9
    • 3
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF)
    Immunogen
    Recombinant human GPD1L (1-351aa) purified from E. coli
    Clone
    AT14E2
    Isotype
    IgG1 kappa
    Top Product
    Discover our top product GPD1L Primary Antibody
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Storage
    4 °C,-20 °C,-80 °C
    Storage Comment
    Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
  • Target
    GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
    Alternative Name
    GPD1L (GPD1L Products)
    Background
    GPD1L is converts sn-glycerol 3-phosphate to glycerone phosphate. This protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). GPD1L is thought to affect trafficking of the cardiac sodium current to the cell surface. Mutations in GPD1L are the cause of sudden infant death syndrome (SIDS) and Brugada syndrome type 2, an autosomal dominant tachyarrhythmia.
    NCBI Accession
    NP_055956
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